meddevicedb.com FDA Device Reference

TUBING CONNECTORS

K860291 Class II Traditional
Decision Date
1986-03-31
Sponsor / Applicant
Biomedical Exports, Inc.

Technical Specification

510(k) Submission ID K860291
Product Code DTL
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4290
Decision Date 1986-03-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TUBING CONNECTORS received FDA 510(k) clearance under submission number K860291, sponsored by Biomedical Exports, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1986-03-31.

Classification & Regulation

This clearance is catalogued under FDA product code DTL and 21 CFR 870.4290, within the Cardiovascular review panel as a Class II device.